Teams at Syneos Health

Designs, analyzes, and interprets real-world evidence studies using EMR and claims data. Develops protocols, data specifications, statistical analysis plans, cohort definitions, causal inference methods, trial emulations, external control arms, and sample size calculations. Collaborates with HEOR, market access, regulatory, and clinical development teams, translating findings into reports and presentations. Requires strong RWE, observational study, healthcare coding, statistical programming, SQL, OMOP, and RWE CMH expertise.

Supports country-level clinical trial site activation, including regulatory and ethics submissions, essential document collection, milestone tracking, financial monitoring, TMF filing, site feasibility, investigator contract and budget support, CTA execution, and coordination among sites, sponsors, and functional teams.

Reviews and evaluates clinical trial data within oncology studies, supporting data quality, consistency, and drug development objectives. Collaborates with clinical solutions and study teams to identify issues, apply therapeutic expertise, and help deliver reliable outcomes for life sciences customers.